Abstract
Ab initio computational methods are employed to explore whether hydrated electrons can be produced by the photodetachment of the excess hydrogen atom of the heptazinyl radical (HzH) in finite-size HzH⋅⋅⋅(H2O)n clusters. The HzH radical is an intermediate species in the photocatalytic oxidation of water with the heptazine (Hz) chromophore. Hz (heptaazaphenalene) is the monomer of the ubiquitous polymeric water-oxidation photocatalyst graphitic carbon nitride (g-C3N4). The energy profiles of minimum-energy excited-state reaction paths for proton-coupled electron transfer from HzH to water molecules were computed for the HzH⋅⋅⋅H2O and HzH⋅⋅⋅(H2O)4 complexes with the CASPT2 method. The results reveal that the photodetachment of the excess H-atom from the HzH radical is a barrierless reaction in these hydrogen-bonded complexes, resulting in the formation of H3O and H3O(H2O)3 radicals, respectively, which are finite-size models of the hydrated electron. The computational results suggest that the photocatalytic formation of hydrated electrons from water with visible light could be possible in principle.
Original language | English |
---|---|
Pages (from-to) | 680-690 |
Number of pages | 11 |
Journal | ChemPhotoChem |
Volume | 5 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2021 |
Keywords
- ab initio calculations
- graphitic carbon nitride
- hydrated electron
- reaction mechanisms
- water oxidation